Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by
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Pharmacovigilance Specialist - Onsite in San Clemente, CA The Pharmacovigilance specialist will report to the Senior manager, Pharmacovigilance. This position will be based in San Clemente, California. This individual is responsible for Post Market and Clinical trial PV Case Processing. This
At AstraZeneca, we deliver life-changing medicines to millions of people globally. Our purpose is ambitious and so is our approach. Crafting a more agile and inclusive environment means building an inspiring culture where we celebrate innovative
Company Description AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives
Get AI-powered advice on this job and more exclusive features. TransPerfect is the world’s largest provider of language and technology solutions for global business. From offices in over 120 cities on six continents, TransPerfect offers a
Director, Global Patient Safety Physician, US About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world’s most serious diseases. But
Title: Pharmacovigilance Specialist Location: Los Angeles, CA 90032 Duration- 4 months (Possible extension for long term) FAQ This position is for Adverse event monitoring. This person will deal with marketed products and side effects, follow up with reporters
COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE! Hybrid work arrangement Medical, Dental, Vision Benefits Health Savings Account (HSA), Flexible Spending Account (FSA) Prescription Drug Coverage Telehealth and Behavior Health Services
Reference Number: JO-2207-496155 Senior Director Medical Affairs Rate: Negotiable Job Type: Permanent Location: Boston Senior Director Medical Affairs, Neurology Location: US, Fully Remote Package: Market leading basic salary, 25% bonus, stock options, long term incentives &
Pharmalex is growing! As a result, we are looking for a PV Manager in Italy to lead projects. We are looking for a strong PV Specialist who is looking for a step up into an oversight role.
Direct message the job poster from Planet Pharma One of our valued Medical Device clients is seeking TA professionals to support their work. Client The client is a medical device company that is using their state-of-the-art
Company Description AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives
Company Description AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and
Company Description Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices. We have a few immediate job opportunities available in
Job Title: PHARMACOVIGILANCE SPECIALIST Job Description The Pharmacovigilance PV Analytics and Reporting Specialist PV Analytics Center of Excellence is responsible for the successful execution and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics
Description Step into a key role at Boehringer Ingelheim as our next Principal Study Coordinator. Drive the integration of patient safety across clinical studies, streamline data processes, and enhance collaboration within our clinical and post-marketing teams.
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and
Proclinical is seeking a Global Labelling Development Lead to guide the labelling development for a key asset and oversee the Target Product Label initiative across our portfolio. Your expertise will also contribute to the labelling strategy